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Evolutionary emergence of infectious diseases in heterogeneous host populations

The emergence and re-emergence of pathogens remains a major public health concern. Unfortunately, when and where pathogens will (re-)emerge is notoriously difficult to predict, as the erratic nature of those events is reinforced by the stochastic nature of pathogen evolution during the early phase o...

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Autores principales: Chabas, Hélène, Lion, Sébastien, Nicot, Antoine, Meaden, Sean, van Houte, Stineke, Moineau, Sylvain, Wahl, Lindi M., Westra, Edze R., Gandon, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171948/
https://www.ncbi.nlm.nih.gov/pubmed/30248089
http://dx.doi.org/10.1371/journal.pbio.2006738
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author Chabas, Hélène
Lion, Sébastien
Nicot, Antoine
Meaden, Sean
van Houte, Stineke
Moineau, Sylvain
Wahl, Lindi M.
Westra, Edze R.
Gandon, Sylvain
author_facet Chabas, Hélène
Lion, Sébastien
Nicot, Antoine
Meaden, Sean
van Houte, Stineke
Moineau, Sylvain
Wahl, Lindi M.
Westra, Edze R.
Gandon, Sylvain
author_sort Chabas, Hélène
collection PubMed
description The emergence and re-emergence of pathogens remains a major public health concern. Unfortunately, when and where pathogens will (re-)emerge is notoriously difficult to predict, as the erratic nature of those events is reinforced by the stochastic nature of pathogen evolution during the early phase of an epidemic. For instance, mutations allowing pathogens to escape host resistance may boost pathogen spread and promote emergence. Yet, the ecological factors that govern such evolutionary emergence remain elusive because of the lack of ecological realism of current theoretical frameworks and the difficulty of experimentally testing their predictions. Here, we develop a theoretical model to explore the effects of the heterogeneity of the host population on the probability of pathogen emergence, with or without pathogen evolution. We show that evolutionary emergence and the spread of escape mutations in the pathogen population is more likely to occur when the host population contains an intermediate proportion of resistant hosts. We also show that the probability of pathogen emergence rapidly declines with the diversity of resistance in the host population. Experimental tests using lytic bacteriophages infecting their bacterial hosts containing Clustered Regularly Interspaced Short Palindromic Repeat and CRISPR-associated (CRISPR-Cas) immune defenses confirm these theoretical predictions. These results suggest effective strategies for cross-species spillover and for the management of emerging infectious diseases.
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spelling pubmed-61719482018-10-19 Evolutionary emergence of infectious diseases in heterogeneous host populations Chabas, Hélène Lion, Sébastien Nicot, Antoine Meaden, Sean van Houte, Stineke Moineau, Sylvain Wahl, Lindi M. Westra, Edze R. Gandon, Sylvain PLoS Biol Research Article The emergence and re-emergence of pathogens remains a major public health concern. Unfortunately, when and where pathogens will (re-)emerge is notoriously difficult to predict, as the erratic nature of those events is reinforced by the stochastic nature of pathogen evolution during the early phase of an epidemic. For instance, mutations allowing pathogens to escape host resistance may boost pathogen spread and promote emergence. Yet, the ecological factors that govern such evolutionary emergence remain elusive because of the lack of ecological realism of current theoretical frameworks and the difficulty of experimentally testing their predictions. Here, we develop a theoretical model to explore the effects of the heterogeneity of the host population on the probability of pathogen emergence, with or without pathogen evolution. We show that evolutionary emergence and the spread of escape mutations in the pathogen population is more likely to occur when the host population contains an intermediate proportion of resistant hosts. We also show that the probability of pathogen emergence rapidly declines with the diversity of resistance in the host population. Experimental tests using lytic bacteriophages infecting their bacterial hosts containing Clustered Regularly Interspaced Short Palindromic Repeat and CRISPR-associated (CRISPR-Cas) immune defenses confirm these theoretical predictions. These results suggest effective strategies for cross-species spillover and for the management of emerging infectious diseases. Public Library of Science 2018-09-24 /pmc/articles/PMC6171948/ /pubmed/30248089 http://dx.doi.org/10.1371/journal.pbio.2006738 Text en © 2018 Chabas et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chabas, Hélène
Lion, Sébastien
Nicot, Antoine
Meaden, Sean
van Houte, Stineke
Moineau, Sylvain
Wahl, Lindi M.
Westra, Edze R.
Gandon, Sylvain
Evolutionary emergence of infectious diseases in heterogeneous host populations
title Evolutionary emergence of infectious diseases in heterogeneous host populations
title_full Evolutionary emergence of infectious diseases in heterogeneous host populations
title_fullStr Evolutionary emergence of infectious diseases in heterogeneous host populations
title_full_unstemmed Evolutionary emergence of infectious diseases in heterogeneous host populations
title_short Evolutionary emergence of infectious diseases in heterogeneous host populations
title_sort evolutionary emergence of infectious diseases in heterogeneous host populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171948/
https://www.ncbi.nlm.nih.gov/pubmed/30248089
http://dx.doi.org/10.1371/journal.pbio.2006738
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